TY - JOUR
T1 - Adsorption of bi-isonicotinic acid on rutile TiO2(110)
AU - Patthey, L.
AU - Rensmo, H.
AU - Persson, P.
AU - Westermark, K.
AU - Vayssieres, L.
AU - Stashans, A.
AU - Petersson, Å
AU - Brühwiler, P. A.
AU - Siegbahn, H.
AU - Lunell, S.
AU - Mårtensson, N.
PY - 1999/3/22
Y1 - 1999/3/22
N2 - Bi-isonicotinic acid (2,2′ -bipyridine-4,4′-dicarboxylic acid) is the ligand of several organometallic dyes, used in photoelectrochemical applications. Therefore the atomic scale understanding of the bonding of this molecule to rutile TiO2(110) should give insight into the crucial dye-surface interaction. High resolution x-ray photoelectron spectroscopy (XPS), near edge x-ray absorption fine structure (NEXAFS), and periodic intermediate neglect of differential overlap (INDO) calculations were carried out on submonolayer bi-isonicotinic acid rutile TiO2(110). Data from multilayers is also presented to support the submonolayer results. For a multilayer, XPS shows that the carboxyl groups remain in the (pristine) protonated form, and NEXAFS show that the molecular plane is tilted by 57° with respect to the surface normal. For the submonolayer, the molecule bonds to the rutile TiO2(110) surface via both deprotonated carboxyl groups, with a tilt angle of 25°, and additionally an azimuthal orientation of 44° with respect to the [001] crystallographic direction. The adsorbant system was also investigated by quantum mechanical calculations using a periodic INDO model. The most stable theoretical adsorption geometry involves a twist around the molecular axis, such that the pyridine rings are tilted in opposite directions. Both oxygen atoms of each carboxyl group are bonded to five-fold coordinated Ti atoms (2M-bidentate), in excellent agreement with the experimental results.
AB - Bi-isonicotinic acid (2,2′ -bipyridine-4,4′-dicarboxylic acid) is the ligand of several organometallic dyes, used in photoelectrochemical applications. Therefore the atomic scale understanding of the bonding of this molecule to rutile TiO2(110) should give insight into the crucial dye-surface interaction. High resolution x-ray photoelectron spectroscopy (XPS), near edge x-ray absorption fine structure (NEXAFS), and periodic intermediate neglect of differential overlap (INDO) calculations were carried out on submonolayer bi-isonicotinic acid rutile TiO2(110). Data from multilayers is also presented to support the submonolayer results. For a multilayer, XPS shows that the carboxyl groups remain in the (pristine) protonated form, and NEXAFS show that the molecular plane is tilted by 57° with respect to the surface normal. For the submonolayer, the molecule bonds to the rutile TiO2(110) surface via both deprotonated carboxyl groups, with a tilt angle of 25°, and additionally an azimuthal orientation of 44° with respect to the [001] crystallographic direction. The adsorbant system was also investigated by quantum mechanical calculations using a periodic INDO model. The most stable theoretical adsorption geometry involves a twist around the molecular axis, such that the pyridine rings are tilted in opposite directions. Both oxygen atoms of each carboxyl group are bonded to five-fold coordinated Ti atoms (2M-bidentate), in excellent agreement with the experimental results.
UR - https://www.scopus.com/pages/publications/0000287782
U2 - 10.1063/1.478491
DO - 10.1063/1.478491
M3 - 文章
AN - SCOPUS:0000287782
SN - 0021-9606
VL - 110
SP - 5913
EP - 5918
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 12
ER -